Canonical Allele Identifier: PA2825614531
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1042329
ClinVar RCV Id: RCV001346263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Thr2142Pro
CA369212745
NM_001127487.2:c.6424A>C